ENST00000209873.9:c.1540G>C
MANE Select
|
ENSP00000209873.4:p.Asp514His
|
|
ENST00000546562.6:n.2604G>C
|
|
|
ENST00000547238.6:n.2176G>C
|
|
|
ENST00000547520.6:n.1656G>C
|
|
|
ENST00000547757.2:c.*458G>C
|
ENSP00000448020.2:n.*458G>C
|
|
ENST00000548931.6:c.975G>C
|
ENSP00000457518.1:p.Met325Ile
|
|
ENST00000549450.6:n.1474G>C
|
|
|
ENST00000672797.1:n.2029G>C
|
|
|
ENST00000209873.8:c.1540G>C
|
ENSP00000209873.4:p.Asp514His
|
|
ENST00000394384.7:c.1441G>C
|
ENSP00000377908.3:p.Asp481His
|
|
ENST00000548931.5:c.975G>C
|
ENSP00000457518.1:p.Met325Ile
|
|
ENST00000550286.5:c.1168G>C
|
ENSP00000446885.1:p.Asp390His
|
|
ENST00000552876.5:n.1883G>C
|
|
|
NM_001173466.1:c.1441G>C
|
NP_001166937.1:p.Asp481His
|
|
NM_015665.5:c.1540G>C
|
NP_056480.1:p.Asp514His
|
|
XM_006719617.2:c.1555G>C
|
XP_006719680.1:p.Asp519His
|
|
XM_011538777.1:c.1597G>C
|
XP_011537079.1:p.Asp533His
|
|
XM_011538778.1:c.1582G>C
|
XP_011537080.1:p.Asp528His
|
|
XM_011538779.1:c.1498G>C
|
XP_011537081.1:p.Asp500His
|
|
XM_011538780.1:c.1483G>C
|
XP_011537082.1:p.Asp495His
|
|
XM_011538781.1:c.931G>C
|
XP_011537083.1:p.Asp311His
|
|
XM_011538778.2:c.1582G>C
|
XP_011537080.1:p.Asp528His
|
|
XM_011538780.2:c.1483G>C
|
XP_011537082.1:p.Asp495His
|
|
XR_001748875.2:n.1597G>C
|
|
|
NM_015665.6:c.1540G>C
MANE Select
|
NP_056480.1:p.Asp514His
|
|
NM_001173466.2:c.1441G>C
|
NP_001166937.1:p.Asp481His
|
|